Canonical Allele Identifier: CA346764669

Gene: FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48050297C>A (hg19) ; chr2:g.47823158C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823158C>A , CM000664.2:g.47823158C>A	GRCh38
NC_000002.11:g.48050297C>A , CM000664.1:g.48050297C>A	GRCh37
NC_000002.10:g.47903801C>A	NCBI36
NG_008397.1:g.87518G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1478G>T
ENST00000682451.1:n.1447G>T
ENST00000682975.1:n.1496G>T
ENST00000683894.1:c.1349G>T	ENSP00000507789.1:p.Ser450Ile
ENST00000684085.1:n.1478G>T
ENST00000684712.1:n.1709G>T
ENST00000403359.8:c.1601G>T MANE Select	ENSP00000384823.4:p.Ser534Ile
ENST00000316377.8:c.1367G>T	ENSP00000323822.5:p.Ser456Ile
ENST00000402508.5:c.1349G>T	ENSP00000385398.1:p.Ser450Ile
ENST00000403359.7:c.1601G>T	ENSP00000384823.3:p.Ser534Ile
ENST00000492225.5:n.1449G>T
ENST00000493962.6:c.975G>T
NM_001190274.1:c.1601G>T	NP_001177203.1:p.Ser534Ile
NM_025133.4:c.1349G>T	NP_079409.3:p.Ser450Ile
XM_005264572.3:c.1601G>T	XP_005264629.1:p.Ser534Ile
XM_005264573.3:c.1598G>T	XP_005264630.1:p.Ser533Ile
XM_005264572.5:c.1601G>T	XP_005264629.1:p.Ser534Ile
XM_005264573.5:c.1598G>T	XP_005264630.1:p.Ser533Ile
XM_017005015.1:c.1598G>T	XP_016860504.1:p.Ser533Ile
XM_017005016.2:c.1349G>T	XP_016860505.1:p.Ser450Ile
XM_017005017.1:c.1349G>T	XP_016860506.1:p.Ser450Ile
NM_001190274.2:c.1601G>T MANE Select	NP_001177203.1:p.Ser534Ile
NM_001374325.1:c.1349G>T	NP_001361254.1:p.Ser450Ile